melissa
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- Joined
- Sep 17, 2006
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Hi everyone!
I'm Melissa, and I just got digital HAs yesterday!
I have mild/moderate loss in the normal (low and speech) frequencies and severe loss in the high frequencies. It's a sensorineural loss I had from birth. Just a bit of background info!
I used to wear analogues when I was younger but I stopped wearing them- they made everything uncomfortably loud.
Today mum called me (quietly) from downstairs and I heard her the first time, she usually has to yell several times. I'd like to hear from other people with digital HAs like myself.
I've just completed a philosophy degree so in this spirit I'm contemplating- I used to tell people I was hoh/hi and to speak up/face me etc but now I'm wearing HAs again I'm not sure what to consider myself. I know labels are best on jars but I don't feel that I identify fully with the hearing or the deaf community. I can get by well without my HAs but people have to repeat things a lot, face me etc. Now I can listen without it being a strain.
Melissa.
I'm Melissa, and I just got digital HAs yesterday!
I have mild/moderate loss in the normal (low and speech) frequencies and severe loss in the high frequencies. It's a sensorineural loss I had from birth. Just a bit of background info!
I used to wear analogues when I was younger but I stopped wearing them- they made everything uncomfortably loud.
Today mum called me (quietly) from downstairs and I heard her the first time, she usually has to yell several times. I'd like to hear from other people with digital HAs like myself.
I've just completed a philosophy degree so in this spirit I'm contemplating- I used to tell people I was hoh/hi and to speak up/face me etc but now I'm wearing HAs again I'm not sure what to consider myself. I know labels are best on jars but I don't feel that I identify fully with the hearing or the deaf community. I can get by well without my HAs but people have to repeat things a lot, face me etc. Now I can listen without it being a strain.
Melissa.